H2-DMalpha(-/-) mice show the importance of major histocompatibility complex-bound peptide in cardiac allograft rejection.
The role played by antigenic peptides bound to major histocompatibility complex (MHC) molecules is evaluated with H2-DMalpha(-/)- mice. These mice have predominantly class II-associated invariant chain peptide (CLIP)-, not antigenic peptide-bound, MHC class II. H2-DMalpha(-/)- donor heart grafts survived three times longer than wild-type grafts and slightly longer than I-A(beta)(b)-(/)- grafts. Proliferative T cell response was absent, and cytolytic response was reduced against the H2-DMalpha(-/)- grafts in vivo. Residual cytolytic T cell and antibody responses against intact MHC class I lead to eventual rejection. Removal of both H2-DMalpha and beta2-microglobulin (beta2m) in cardiac grafts lead to greater (8-10 times) graft survival, whereas removal of beta2m alone did not have any effect. These results demonstrate the significance of peptide rather than just allogeneic MHC, in eliciting graft rejection.
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Related Subject Headings
- Transplantation, Homologous
- Th2 Cells
- Th1 Cells
- Myocardium
- Mice, Knockout
- Mice, Inbred Strains
- Mice, Inbred DBA
- Mice, Inbred BALB C
- Mice
- Major Histocompatibility Complex
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Transplantation, Homologous
- Th2 Cells
- Th1 Cells
- Myocardium
- Mice, Knockout
- Mice, Inbred Strains
- Mice, Inbred DBA
- Mice, Inbred BALB C
- Mice
- Major Histocompatibility Complex